Treatment of Neurocutaneous Syndrome, Including Compositions, Methods and Uses Thereof

A treatment protocol for use in the treatment of neurocutaneous syndrome is described and comprises at least one xanthone component, which may comprise at least one mangosteen component, and at least one detoxification component. Additional embodiments comprise at least one herbal component, at least one vitamin component, or a combination thereof. A method of treating a patient having neurocutaneous syndrome is described herein and comprises: providing at least one xanthone component, which may comprise at least one mangosteen component, providing at least one xanthone component, which may comprise at least one mangosteen component, to the patient, and administering the at least one detoxification component to the patient. Additional methods steps may include providing and administering at least one herbal component, providing and administering at least one vitamin component or a combination thereof.

Skip to: Description  ·  Claims  · Patent History  ·  Patent History
Description
FIELD OF THE SUBJECT MATTER

The field of the subject matter is treatment of neurocutaneous syndrome, which is also known as Morgellons, including the compositions, methods and uses thereof.

BACKGROUND

The terms “Morgellons” and “Neurocutaneous Syndrome” or NCS, as characterized by Dr. Omar Amin (2001-2009), are used interchangeably, yet cautiously, as their symptoms are very similar. While the etiological agent(s) and remedies of Morgellons have never been identified, these factors for NCS have been well-researched and published in refereed medical journals (see References Cited Section herein), and patients have been successfully helped.

Researchers in this area have recognized that patients experience dermatological abnormalities (elevated itchy skin sores that may develop into mucoid lesions) and neurological symptoms (movement, pin prick or crawling sensations) caused by toxic exposures to a wide variety of environmental factors. Those factors include, but are not limited to, incompatible dental materials, toxic fumes in the work place, insecticides or allergenic sprays, household chemicals, implants, recreational drugs, e.g., crystal methamphetamine and/or cocaine, medications, creams, hot sulfur/mineral springs, and any other environmental exposures to which the patient is allergic.

To date, no one has been able to develop and utilize a treatment protocol, including components and supplements directed specifically to treating NCS and the symptoms related to NCS. To this end, it would be desirable to develop, produce and utilize a formulation, formulations and related protocols that can easily and effectively treat NCS and the related symptoms, while at the same time minimizing pain and discomfort of the patient.

SUMMARY OF THE SUBJECT MATTER

A treatment protocol for use in the treatment of neurocutaneous syndrome is described and comprises at least one xanthone component, which may include at least one mangosteen component, and at least one detoxification component. Additional embodiments comprise at least one herbal component, at least one vitamin component, or a combination thereof.

A method of treating a patient having neurocutaneous syndrome is described herein and comprises: providing at least one xanthone component, which may include at least one mangosteen component, providing at least one detoxification component, administering the at least one xanthone component to the patient, and administering the at least one detoxification component to the patient. Additional methods steps may include providing and administering at least one herbal component, providing and administering at least one vitamin component or a combination thereof.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows a contemplated method for the treatment of neurocutaneous syndrome, comprising a method 100 of treating a patient having neurocutaneous syndrome comprises: providing at least one xanthone component 110, which may include at least one mangosteen component, providing at least one detoxification component 120, administering the at least one xanthone component to the patient 130, and administering the at least one detoxification component to the patient 140. Additional methods steps may include providing and administering at least one herbal component, providing and administering at least one vitamin component or a combination thereof 150.

FIG. 2 shows a contemplated method for the treatment of neurocutaneous syndrome, comprising a method 200 of treating a patient having neurocutaneous syndrome comprises: providing at least one mangosteen component 210, providing at least one detoxification component 220, administering the at least one mangosteen component to the patient 230, and administering the at least one detoxification component to the patient 240. Additional methods steps may include administering a targeted questionnaire 250, administering a blood bio-compatibility test 260, administering massage therapy to the patient 270, which may include lymph drainage massage therapy, providing and administering at least one herbal component, providing and administering at least one vitamin component or a combination thereof (shown in FIG. 1), or a combination thereof.

DETAILED DESCRIPTION

As described herein, a successful treatment protocol, including components and supplements directed specifically to treating NCS and the symptoms related to NCS has been developed. The Examples section will provide a detailed example of a contemplated treatment protocol and additional component parts. As also will be described herein, formulation, formulations and related protocols and methods that can easily and effectively treat NCS and the related symptoms, while at the same time minimizing pain and discomfort of the patient, have been developed and are being successfully utilized in practice.

Specifically, a treatment protocol for use in the treatment of neurocutaneous syndrome comprises at least one xanthone component, which may include at least one mangosteen component, and at least one detoxification component. Additional embodiments comprise at least one herbal component, at least one vitamin component, or a combination thereof.

In addition, and as shown in FIG. 1, a method 100 of treating a patient having neurocutaneous syndrome comprises: providing at least one xanthone component 110, which may include at least one mangosteen component, providing at least one detoxification component 120, administering the at least one xanthone component to the patient 130, and administering the at least one detoxification component to the patient 140. Additional methods steps may include providing and administering at least one herbal component, providing and administering at least one vitamin component or a combination thereof 150.

As shown in FIG. 2, a method 200 of treating a patient having neurocutaneous syndrome comprises: providing at least one mangosteen component 210, providing at least one detoxification component 220, administering the at least one mangosteen component to the patient 230, and administering the at least one detoxification component to the patient 240. Additional methods steps may include administering a targeted questionnaire 250, administering a blood bio-compatibility test 260, administering massage therapy to the patient 270, which may include lymph drainage massage therapy, providing and administering at least one herbal component, providing and administering at least one vitamin component or a combination thereof (shown in FIG. 1), or a combination thereof.

Treatment protocols and methods of treating patients, as disclosed herein, include at least one xanthone component, which may include at least one mangosteen component. The mangosteen fruit, particularly the rind, or pericarp, has been used in traditional folk medicine for centuries. It is well known in Asia, where it is often called “The Queen of Fruits”, but is unavailable in the United States. Folk medicine has long used the mangosteen peel for a variety of ailments, used differently in different parts of Asia. As disclosed herein, the “at least one mangosteen component” refers to the extract of the fruit, the extract of the rind, the fruit, the juice from the fruit, the rind, or a combination thereof.

Research scientists are now discovering that there is valid science behind the folk medicine traditions and the answer seems to be in the mangosteen's compounds called xanthones. There have been 43 xanthones discovered in the fruit thus far (mostly in the rind); some unique only to the mangosteen. Xanthones are potent anti-oxidants and are used for their anti-toxic benefits; they have been found to have potent anti-inflammatory, anti-bacterial, anti-viral, anti-tumor and anti-fungal properties; they help with neurological and cardiovascular disorders and have other healing properties as well. These properties have prompted health professionals to utilize the mangosteen in a variety of conditions, including pain, gastrointestinal problems, dermatologic diseases (including eczema, skin sores and lesions, etc.), musculoskeletal conditions, dental/oral disorders and much more. The mangosteen is one of nature's only readily available sources of xanthones known thus far. In contemplated embodiments, the xanthone component or the mangosteen component may be administered in any suitable amount, depending on the needs of the patient, in order to treat NCS. Amounts that are not suitable to treat NCS are not contemplated herein.

Additionally, mangosteen was used traditionally for its anti-parasitic effects: Malaria, amoebic dysentery and syphilis are caused by parasites. Asian healers have used mangosteen for centuries to deal with those illnesses. In South America, mangosteen is also used to cure intestinal worm infestations. Laboratory research to confirm these practices, however, is not yet available at this time.

As disclosed, contemplated treatment protocols and methods of treating patients include at least one detoxification component. In some embodiments, the detoxification component may either be or comprise a mangosteen component. In other embodiments, the at least one detoxification component may comprise additional components other than mangosteen or its derivatives.

Contemplated treatment protocols and methods of treating patients with parasitic infections may also include providing and utilizing at least one of the following herbal components in a suitable amounts: Oregano Leaf, Clove Flower, Black Walnut Husk, Peppermint Leaf, Black Cumin Seed, Winter Melon Seed, Gentian Root, Wormwood Bark, Hyssop Leaf, Cramp Bark, Thyme Leaf, Fennel Seed, Pumpkin Seed, Caprylic Acid, Pagoda Fruit, Rosemary, Aloe Vera, Betel Nut Palm, Papaya, Citrus Extract, Pomegranate, Rangoon Creeper, Tansy, Psyllium Seed Husk, Atlantic Kelp, Corn Silk, Fo-Ti, Chinese Rhubarb, Black Cumin Seed, Cinnamon Bark, Fennel Seed, Ginger Root, Orange Peel Extract, Clove Bulb, Cascara Sagrada, Slippery Elm Bark, Molasses, Carob, Rhubarb Root, Thyme Leaf, Clove Bulb, Cayenne Fruit, Rosemary Leaf, Alfalfa Leaf, Licorice Root, Chamomile, Grapefruit Seed, Echinacea, Chicory Root, Corn Silk, Safflower Oil Powder, Sage or a combination thereof. In some contemplated embodiments, a combination of at least some of these components is packaged in three anti-parasitic formulas that may be referred to as “Freedom/Cleanse/Restore”. Contemplated detoxification formulas and products that can be utilized as at least part of the at least one herbal component includes a HEEL Detox kit, Ubichinon, Coenzyme or a combination thereof, all of which are manufactured by HEEL USA. It should be understood that other components and methods of detoxification can also be used.

Contemplated treatment protocols and methods of treating patients may also include providing and utilizing at least one vitamin component, which includes or may include one or more of the following components or ingredients in a suitable amount: vitamin B (all forms, including vitamin B12, B5 and B6), folic acid, minerals, such as zinc, calcium, magnesium oxide or citrate, vitamin E, vitamin C, Omega oils (including Omega 3 fish oil or lin seed oil), acidofilus, bifidus, lactobacillus, amino acids, digestive enzymes, selenium and L-glutathione. A contemplated daily dose of the at least one vitamin component may include:

    • Vitamin B12: 1-2 mg (methycobalamin)
    • Vitamin 86: 100 mg (pyridokal-5-phosphate)
    • Folic Acid: 200-300 mcg
    • Zinc: 30-50 mg
    • Vitamin E: 300-500 IU (dl-alpha tocopheryl acetate)
    • Vitamin B5: 500 mg (pantothenic acid)

Calcium: 200-400 mg (not carbonate)

    • Magnesium Oxide or Citrate: 300-500 mg
    • Time release Vitamin C: 1000-3000 mg
    • Omega 3 fish oil or lin seed oil
    • Acidofilus, Bifidus, Lactobacillus
    • Amino Acids
    • Digestive Enzymes
    • Selenium: 100-200 mcg
    • L Glutathione: 100-150 mg (50-250, suitable)

All patients that comply, at least partly and ideally fully, with contemplated embodiments and programs have recovered. Neurocutaneous Syndrome (NCS), a newly discovered toxicity syndrome is characterized by neurological and dermatological disorders as well as systemic and related dysfunctions.

As disclosed earlier, patients experience, among other symptoms, pin-prick movement sensations and in later stages, itchy cutaneous lesions that may invite various opportunistic infections (insects, worms, fungus, pathogenic bacteria, among others) often confused as causative agents of the syndrome.

The toxicity of dental chemicals, compounding factors and case histories were discussed and management protocols researched at the Parasitology Center, Inc. (PCI) were proposed. Components of calcium hydroxide sealants and liners (Dycal, Life, and Sealapex) and at least 644 other dental chemicals, have been identified as a source of the observed symptoms. NCS patients often confuse the movement sensations, itchy skin and related symptoms with parasitic infections and seek medical help under this assumption. Invariably, they are diagnosed with and treated for other etiologies often including arthropod infestation and/or mental conditions such as psychosis and delusional parasitosis. Patients are genuine clinical cases who should not be further compromised by inaccurate diagnosis, wrongly medicated or subjected to psychological treatment in mental health care facilities.

EXAMPLES Example 1 A Contemplated Treatment Protocol

A contemplated treatment protocol has been developed and designed to identify, analyze, treat and follow-up with a patient who has neurocutaneous syndrome or NCS. It should be understood that many of the components and methods disclosed herein are incorporated in this Example, along with other desirable components and methods steps.

A Protocol for NCS Rehabilitation

    • Interviewing the patient.
    • Examining patient and verifying symptoms, history, and the presence of toxic dental materials. Documenting dermatological symptoms with photos.
    • Examinating dental and related records.
    • Administering a targeted questionnaire to the patient.
    • Documenting symptoms, dates and history.
    • Swabbing patient's skin for culture of bacteriological and fungal infections.
    • Establishing a diagnosis and providing a diagnostic report to patient.
    • Referring patient to a holistic dentist in patient's area of residence.
    • Initiating blood dental-bio compatibility testing.
    • Identifing compromised teeth and begin treatment; no more than 3 teeth restored in one month.
    • Supplementing with the at least one vitamin component during treatment; symptoms will get worse before they get better.
    • Making recommendations for additional nutritional remedies.
    • Initiating detoxification of organ systems by utilizing the at least one herbal component.
    • Instituting lymph drainage massage therapy, and laser therapy if needed.
    • Following up with patient.

The first three steps of the above-referenced protocol are self-explanatory and should be understood by anyone who is trained in dentistry or is a trained physician. The next step includes administering a targeted questionnaire to the patient. A contemplated questionnaire is found below.

NCS Questionnaire

Mark the intensity of the following symptoms on a scale of 1-3. 1, mild, 2; moderate, 3; severe.

Use approximate date for “first observed” and use N/A, occasionally, often, and always for frequency.

Based on the protocol outlined above, along with the responses to the Questionnaire outlined herein, a detailed analysis of the clinical history of a random sample of 50 NCS patients (9 males, 41 females) was reported.

Symptoms were classified into six categories, neurological (sensory imbalances), dermatological (including opportunistic skin infections), systemic, oral, allergic and general. The most common symptoms in each of these categories in the same order are pin prick and crawling sensations, skin lesions and sores, respiratory and bowel disturbances, gum disease, sensitivities to light, noise and mold, and fatigue and insomnia. Symptoms were relatively similar in both sexes. These results were tabulated and their biological foundation explained. The misdiagnosis of NCS cases by medical professionals is discussed. NCS symptoms in toothless patients or those with dentures, and those on recreational drugs are described. Initially, over 360 dental toxins are placed in four major categories and their mode of action explained. Incubation period varied between a few hours to 28 years. Our protocol for rehabilitation is included. All patients following and completing our rehabilitation program have invariably recovered.

Early reports on this syndrome included the description of a case with many facial opportunistic infections from Oklahoma and the first naming and evaluation of the syndrome from three more cases, with a special reference to fibers and springtails (Collembola). By 2003, a comprehensive evaluation of NCS and establish the link to dental toxins as the causative agents was able to be provided. Amin clarified the nature of action of dental liners (bases) in the causation of NCS neurological and dermatological symptoms and provided the history of three NCS patients who have recovered following rehabilitation thus establishing a cause-effect relationship. Various versions of this landmark publication were subsequently published.

The above contributions were researched and published, and patients were successfully helped long before we discovered a similar clinical entity called Morgellons. The only difference is that we have done the research, established a causal relationship with dental toxins, developed a protocol, and successfully helped patients.

Most people have had dental work. Many have various degrees of sensitivity to some dental materials to which their bodies manifest varied intensities of symptoms. This epidemic-in-disguise has been routinely misunderstood by medical professionals who often label patients as delusional because of their unfortunate description of their neurological symptoms (actually caused by nerve damage) as having been caused by parasite infections. Amin specifically addressed this issue while discussing the clinical history of 24 NCS patients.

Of these patients, seven who have followed and completed the contemplated and disclosed protocol have experienced full recovery.

Amin provided an annotated list of about 400 dental materials that have been involved in the causation of NCS symptoms in patients that we have studied. Toxic ingredients common to all listed chemicals were classed in four categories. These categories are found in many more dental chemicals that were not reported in Amin's preliminary list. An overview of NCS made special reference to organ system symptomology in 50 patients of both sexes and all age groups, misdiagnoses, storage organs, sealants, drug involvement, incubation period, and recovery, with the discussion of five relevant cases. The personal perspectives of patients who have recovered from NCS have been presented by themselves.

Thus, specific embodiments, protocols and methods of the treatment of neurocutaneous syndrome have been disclosed. It should be apparent, however, to those skilled in the art that many more modifications besides those already described are possible without departing from the inventive concepts herein. The inventive subject matter, therefore, is not to be restricted except in the spirit of the disclosure herein. Moreover, in interpreting the specification and claims, all terms should be interpreted in the broadest possible manner consistent with the context. In particular, the terms “comprises” and “comprising” should be interpreted as referring to elements, components, or steps in a non-exclusive manner, indicating that the referenced elements, components, or steps may be present, or utilized, or combined with other elements, components, or steps that are not expressly referenced.

REFERENCES CITED

  • Amin, O. M. 1996. Facial cutaneous dermatitis associated with arthropod presence Explore! for the professional 7:62-64, incorporated herein in its entirety by reference.
  • Amin, O. M. 2001. Neuro-cutaneous Syndrome (NCS): a new disorder. Explore! for the Professional 10:55-56, incorporated herein in its entirety by reference.
  • Amin, O. M. 2003. On the diagnosis and management of Neuro-cutaneous Syndrome (NCS), a toxicity disorder from dental sealants. Explore! for the Professional 12:21-25, incorporated herein in its entirety by reference.
  • Amin, O. M. 2004 b. On the course of Neuro-cutaneous Syndrome (NCS) and its pseudo-diagnosis by medical professionals. Explore! for the Professional 13:4-9, incorporated herein in its entirety by reference.
  • Amin, O. M. 2006 b. An Overview of Neuro-cutaneous Syndrome (NCS) with a special reference to symptomology. Explore! for the Professional 15: 41-49, incorporated herein in its entirety by reference.
  • Amin, O. M. 2007. The face of Neuro-cutaneous Syndrome (NCS): new cases, recovery, and perspectives. Explore! for the Professional 16: 54-64, incorporated herein in its entirety by reference.
  • Keleher, J. W. 2008. Hell and Back Again, and Account of Morgellons Disease and it's Cure From a Former Sufferer. Explore! for the Professional 17: 14-16.
  • Amin, O. M. 2009 Recovering from Morgellons and Neuro-cutaneous Syndrome (NCS): Patients & Perspectives. Explore for the Professional. 18:1-8, incorporated herein in its entirety by reference.
  • Amin, O. M.2010 In Their Own Words or: Symptoms of Morgellons and Neuro-Cutaneous Syndrome (NCS) Upon First Examination at the Parasitology Center, Inc. (PCI) 19: 1-8, incorporated herein in its entirety by reference.
  • Amin, O. M. 2012 A Comprehensive Study of Dental Materials and Their Toxic Ingredients Associated with Neuro-Cutaneous Syndrome (NCS) and Morgellons, with Notes on Research Background. Explore! 21.1:14-23, incorporated herein in its entirety by reference.
  • Moongkarndi, P. et al. Antiproliferation, Antioxidation and Induction of Apoptosis by Garcinia Mangostana (Mangosteen) on SKBR3 Human Breast Cancer Cell Line. J. Ethnopharmacol. 2004; 90 (1):161-6.
  • Nakatani, K. et al. Inhibition of Cyclooxygenase and Prostaglandin E2 Synthesis by Gamma-Mangostin, a Xanthone Derivative in Mangosteen, in C6 Rat Glioma Cells. Biochem Pharmacol. 2002 Jan. 1; 63(1):73-9.
  • Sakagami, Y. et al. Antibacterial Activity of Alpha-Mangostin against Vancomycin Resistant Enterococci (VRE) and Synergism with Antibiotics. Phytomedicine. 2005; 12(3):203-8.
  • Chen, S X. Active Constituents against HIV-1 Protease from Garcinia Mangostana. Planta Med 1996; 62 (4) 381-2.
  • Nabandit, V. et al. Inhibitory Effects of Crude Alpha Mangostin, a Xanthone Derivative, on Two Different Categories of Colon Preneoplastic Lesions Induced by 1, 2-dimethylhydrazine in the Rat. Asian Pac J. Cancer Prey. 2004; 5(4):433-8.
  • Dharmaratne, H R et al. A Geranylated Biphenyl Derivative from Garcinia Mangostana. Nat. Prod. Res. 2005 April; 19(3): 239-43.
  • Nakatani, K. et al. Gamma Mangostin Inhibits Kinase Activity and Decreases Lipopolysaccharide-Induced Cyclooxygenase-2 Gene Expression in C6 Rat Glioma Cells. Molecular Pharmacol. September 2004; 66(3)667-674.
  • Jiang, D J et al. Pharmacological Effects of Xanthones as Cardiovascular Protective Agents. Cardiovascular Drug Rev. 2004; 22 (2):91-102.
  • Nakatani, K. et al. Inhibitions of Histamine Release and Prostaglandin E2 Synthesis by Mangosteen, a Thai Medicinal Plant. Biol. Pharm Bull. 2002; 25 (9):1 137-41.
  • Begum, N, et al. Anti-ulcer and Antimicrobial Activities of Gartanin, a Xanthone from Garcinia Mangostana Linn. Bulletin Islam. 1982; 2 (20) 518-521.
  • Templeman, J. Frederick, Mangosteen, The X-Factor. Volume 3, pp. 37-38.
  • Templeman, J. Frederick, Mangosteen, The X-Factor. Volume 3, pp. 14-18.
  • Templeman, J. Frederick, Mangosteen, The X-Factor. Volume 3, Preface.

Claims

1-20. (canceled)

21. A treatment protocol for use in the treatment of neurocutaneous syndrome comprising:

administering to a patient in need thereof, at least one xanthone component;
and administering to a patient in need thereof, at least one detoxification component wherein the at least one detoxification component comprises berberis-homaccord, lyphosot, flux vomica-homaccord, ubichinon, ubicoenzyme or a combination thereof.

22. The treatment protocol of claim 21, further comprising administering to a patient in need thereof, at least one herbal component, at least one vitamin component, or a combination thereof.

23. The treatment protocol of claim 21, wherein the at least one xanthone component comprises at least one mangosteen component.

24. The treatment protocol of claim 23, wherein the at least one mangosteen component comprises an extract of a mangosteen fruit.

25. The treatment protocol of claim 23, wherein the at least one mangosteen component comprises a suitable amount of the extract of the mangosteen fruit.

26. The treatment protocol of claim 23, wherein the at least one mangosteen component comprises mangosteen juice.

27. The treatment protocol of claim 22, wherein the at least one herbal component comprises Oregano Leaf, Clove Flower, Black Walnut Husk, Peppermint Leaf, Black Cumin Seed, Winter Melon Seed, Gentian Root, Wormwood Bark, Hyssop Leaf, Cramp Bark, Thyme Leaf, Fennel Seed, Pumpkin Seed, Caprylic Acid, Pagoda Fruit, Rosemary, Aloe Vera, Betel Nut Palm, Papaya, Citrus Extract, Pomegranate, Rangoon Creeper, Tansy, Psyllium Seed Husk, Atlantic Kelp, Corn Silk, Fo-Ti, Chinese Rhubarb, Black Cumin Seed, Cinnamon Bark, Fennel Seed, Ginger Root, Orange Peel Extract, Clove Bulb, Cascara Sagrada, Slippery Elm Bark, Molasses, Carob, Rhubarb Root, Thyme Leaf, Clove Bulb, Cayenne Fruit, Rosemary Leaf, Alfalfa Leaf, Licorice Root, Chamomile, Grapefruit Seed, Echinacea, Chicory Root, Corn Silk, Safflower Oil Powder, Sage or a combination thereof.

28. The treatment protocol of claim 22, wherein the at least one vitamin component comprises vitamin B, folic acid, minerals, such as zinc, calcium, magnesium oxide or citrate, vitamin E, vitamin C, Omega oils, acidofilus, bifidus, lactobacillus, amino acids, digestive enzymes, selenium, L-glutathione or a combination thereof.

Patent History
Publication number: 20130202570
Type: Application
Filed: Sep 20, 2012
Publication Date: Aug 8, 2013
Inventor: Omar M. Amin (Scottsdale, AZ)
Application Number: 13/623,558
Classifications
Current U.S. Class: Lactobacillus Or Pediococcus Or Leuconostoc (424/93.45); Chalcogen Bonded Directly To Ring Carbon Of The Hetero Ring (514/455); Containing Or Obtained From Labiatae (e.g., Oregano, Marjoram, Etc.) (424/745); Plant Material Or Plant Extract Of Undetermined Constitution As Active Ingredient (e.g., Herbal Remedy, Herbal Extract, Powder, Oil, Etc.) (424/725); Oak, Maple, Walnut, Ash, Poplar, Dogwood, Or Persimmon (424/771); Containing Or Obtained From Mentha (e.g., Mint, Peppermint, Spearmint, Habak, Etc.) (424/747); Containing Or Obtained From Cucumbrits (e.g., Gourds Such As Pumpkin, Squash, Cucumber, Etc.) (424/758); Containing Or Obtained From Artemisia (e.g., Wormwood, Absinthe, Etc.) (424/740); Containing Or Obtained From Leguminosae (e.g., Legumes Such As Soybean, Kidney Bean, Pea, Lentil, Licorice, Etc.) (424/757); Containing Or Obtained From Aloe (e.g., Aloe Vera, Etc.) (424/744); Containing Or Obtained From Palmaceae (e.g., Date, Coconut, Saw Palmetto, Etc.) (424/727); Containing Or Obtained From Citrus (e.g., Orange, Lemon, Lime, Grapefruit, Etc.) (424/736); Containing Or Obtained From Plantago (e.g., Plantain, Psyllium, Etc.) (424/738); Extract Or Material Containing Or Obtained From An Alga As Active Ingredient (e.g., Chlorella, Seaweed, Laver, Kelp, Etc.) (424/195.17); Containing Or Obtained From Gramineae (e.g., Bamboo, Corn, Or Grasses Such As Grain Products Including Wheat, Rice, Rye, Barley, Oat, Etc.) (424/750); Containing Or Obtained From Cinnamomum (e.g., Cinnamon, Etc.) (424/739); Containing Or Obtained From Zingiberaceae (e.g., Afromonun, Cardemon, Ginger, Turmeric, Etc.) (424/756); Containing Or Obtained From Compositeae (e.g., Marigold, Sunflower, Dandelion, Feverfew, Yarrow, Chamomile, Etc.) (424/764); Containing Or Obtained From Salvia (e.g., Sage, Etc.) (424/746); Orally Assimilable Or Injectable Composition (424/643); Aluminum, Calcium Or Magnesium Element, Or Compound Containing (424/682); Magnesium Hydroxide Or Oxide (424/692); Enzyme Or Coenzyme Containing (424/94.1); Selenium Or Compound Thereof (424/702)
International Classification: A61K 31/352 (20060101); A61K 36/61 (20060101); A61K 36/52 (20060101); A61K 36/534 (20060101); A61K 36/71 (20060101); A61K 36/42 (20060101); A61K 36/515 (20060101); A61K 36/282 (20060101); A61K 36/235 (20060101); A61K 36/48 (20060101); A61K 36/886 (20060101); A61K 36/889 (20060101); A61K 36/752 (20060101); A61K 36/68 (20060101); A61K 36/02 (20060101); A61K 36/899 (20060101); A61K 36/54 (20060101); A61K 36/906 (20060101); A61K 36/484 (20060101); A61K 36/28 (20060101); A61K 36/537 (20060101); A61K 33/30 (20060101); A61K 33/06 (20060101); A61K 33/08 (20060101); A61K 35/74 (20060101); A61K 38/43 (20060101); A61K 33/04 (20060101); A61P 25/00 (20060101); A61K 36/53 (20060101);